A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238058



Internal ID20805098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49140132..49141437hg38UCSC Ensembl
chr15:49432329..49433634hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595270
Supporting Variants
Samples
Known GenesCOPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238058
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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